This product is intended for in vitro diagnostic use in the quality control of serum on clinical chemistry systems.

This product is intended for in vitro diagnostic use in the quality control of serum on clinical chemistry

The Direct Bilirubin test system is a device intended for the quantitative in vitro determination of Direct Bilirubin in serum and plasma.

For the quantitative in vitro determination of Total Bilirubin in serum and plasma.

The device is intended for the quantitative in vitro determination of carbon dioxide in serum or plasma.

Enzymatic Clearance assay for the in vitro quantitative determination of LDL-cholesterol in human serum and plasma.

The device is intended for the quantitative in vitro determination of CK-MB concentration in serum or plasma.

Intended for use with the Ion Selective Electrode unit for measuring concentration of electrolytes in the blood serum, plasma or urine.

Intended for use with the Ion Selective Electrode unit for measuring concentration of electrolytes in the blood serum, plasma or urine.

Intended for use with the Ion Selective Electrode unit for measuring concentration of electrolytes in the blood serum, plasma or urine.

Intended for use with the Ion Selective Electrode unit for measuring concentration of electrolytes in the blood serum, plasma or urine.

Intended for use with the Ion Selective Electrode unit for measuring concentration of electrolytes in the blood serum, plasma or urine.

Intended for use with the Ion Selective Electrode unit for measuring concentration of electrolytes in the blood serum, plasma or urine.

Intended for use with the Ion Selective Electrode unit for measuring concentration of electrolytes in the blood serum, plasma or urine.

Intended for use with the Ion Selective Electrode unit for measuring concentration of electrolytes in the blood serum, plasma or urine.

Used as a Calibrator in a two-point calibration. L Solution is pumped into the sample port by the L Solution pump and then positioned in front of the sensor.

The RANDOX evidence® system is a fully automated, continuous access immunoanalyser using protein biochip array technology. It is intended for the in-vitro qualitative, semi-quantitative or fully quantitative determination of various diagnostic markers.

This product is intended for in vitro diagnostic use, in the quality control of the accuracy of Glycated Haemoglobin (HbA1c) on clinical chemistry systems.

This product is intended for in vitro diagnostic use, in the quality control of diagnostic assays. The Liquid Assayed Chemistry Control Premium Plus is for the control of accuracy.

The Reagent Precision Test is used on the RX series clinical chemistry systems for checking proper functioning of the reagent fluid metering and photometric measuring system.

This should be run once a day to prevent protein build up or at 8 hour intervals if the ISE module performs more than 50 samples per day. Cleaning solution may be aspirated from a sample cup but the cup must be covered between use to eliminate evaporation and ensure accuracy.

Used as a Calibrator in a two-point calibration. L Solution is pumped into the sample port by the L Solution pump and then positioned in front of the sensor.

This is required for measuring reference electrode potential of an ion selective electrode module.

Used as a Calibrator in a two-point calibration. H Solution is aspirated from a sample cup located in a pre-registered position on the sample carousel.

The product should be run on a weekly basis to prevent protein build up.

This should be run on a weekly basis to prevent protein build up.

The product is intended for use in the measurement of urine samples.

Antibacterial Detergent is used for cleaning the instrument probe and reaction cuvettes.

Alkaline Detergent is used for cleaning the instrument probe and reaction cuvettes.

Acid Wash Solution should be used in conjunction with reagents to clean probes and cuvettes

Alkaline Wash Solution should be used in conjunction with reagents to clean cuvettes

The Precision Check Solution is used for checking proper functioning of the reagent and sample fluid metering and photometric measuring system.

This product is a weak bleach solution.

This product is intended for in vitro diagnostic use, in the calibration of the Randox Ransel assay.

This product is used for checking proper functioning of the sample fluid metering system as well as the photometric measuring system.

A TIBC_2 test system is a device intended for the quantitative in vitro determination of total iron-binding capacity (TIBC) concentration in serum.

A TIBC_2 test system is a device intended for the quantitative in vitro determination of total iron-binding capacity (TIBC) concentration in serum.

For the quantitative in vitro determination of Triglycerides in serum.

This product is intended for the quantitative in vitro determination of Urea in serum, plasma or urine.

This product should be used in conjunction with RX daytona plus reagents to clean probes and cuvettes.